Dietary treatment of homocystinuria.

Author:

Komrower G. M.,Lambert A. M.,Cusworth D. C.,Westall R. G.

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Homocystinuria: clinical and dietary studies;Brenton, D.P.; Cusworth, D.C.; Dent, C.E.; Jones, E.E.;Quart. J'. Med,1966

2. Homocystinuria. Biochemical studies of tissues including a comparison with cystathioninuria;Gaull, G.E.;Pediatrics,1965

3. Homocystinuria: a new inborn error of metabolism associated with mental deficiency;Carson, N.A.J.; Cusworth, D.C.; Dent, C.E.; Field, C.M.B.; Neill, D.W.; Westall, R.G.;Arch. Dis. Childh,1963

4. Homocystinuria. A new disorder of metabolism. Abstr;Field, C.M.B.; Carson, N.A.J.; Cusworth, D.C.; Dent, C.E.; Neill, D.W.;Cong. Paediat., Lisbon,1962

5. Homocystinuria due to cystathionine synthetase deficiency: the mode of inheritance;Finkelstein, J.D.; Mudd, S.H.; Irreverre, F.; Laster, L.;Science,1964

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